Package 63629-8759-1

Brand: potassium citrate

Generic: potassium citrate
NDC Package

Package Facts

Identity

Package NDC 63629-8759-1
Digits Only 6362987591
Product NDC 63629-8759
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8759-1)

Marketing

Marketing Status
Marketed Since 2022-08-25
Brand potassium citrate
Generic potassium citrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3af62a61-a384-4f52-aa75-6419fea90b54", "openfda": {"unii": ["EE90ONI6FF"], "rxcui": ["199381"], "spl_set_id": ["4af19ffc-80e1-4182-bccf-e7abb1bf457c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8759-1)", "package_ndc": "63629-8759-1", "marketing_start_date": "20220825"}], "brand_name": "Potassium Citrate", "product_id": "63629-8759_3af62a61-a384-4f52-aa75-6419fea90b54", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "63629-8759", "generic_name": "Potassium Citrate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Citrate", "active_ingredients": [{"name": "POTASSIUM CITRATE", "strength": "10 meq/1"}], "application_number": "ANDA209758", "marketing_category": "ANDA", "marketing_start_date": "20180530", "listing_expiration_date": "20261231"}